Echo-guided Scalp Blocks and Incidence of Postoperative Pain in Scheduled Supratentorial Intracranial Surgery.

Trial statusNot yet recruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity Hospital, Bordeaux

About this trial

Up to 30% of patients undergoing intracranial surgery present moderate to severe pain. In this type of surgery, the restriction of the pharmacopoeia, which goes against the concept of multimodal analgesia, results in the important use of opioids not without consequences in terms of complications. Numerous studies have highlighted the benefits of scalp blocks in postoperative pain. The originality of this study lies firstly in the fact that the scalp blocks will be guided by ultrasound and secondly, the incidence of severe pain after scalp blocks will be evaluated

Eligibility criteria

Qualifiers

Patient managed in the neurosurgical unit for supratentorial intracranial surgery.

Person affiliated or beneficiary of a social security plan.

Free, informed, and written consent signed by the participant and the investigating physician (at the latest on the day of inclusion and before any examination required by the research).

Disqualifiers

Surgical procedure under awake surgery (systematic realization of scalp blocks necessary)

Aphasia of comprehension preoperatively or expected postoperatively or any other neurological impairment making self-evaluation of pain impossible.

Contraindication to the use of local anesthetics: allergy or history of intoxication to local anesthetics

Contraindication to adrenaline infiltration: severe ventricular rhythm disorders, severe obstructive cardiomyopathy, unstable coronary insufficiency, hypersensitivity to adrenaline.

Trial design

Treatments tested in this trial

  • Echo-guided scalp blocks
  • Classic anesthetic strategy

Treatment groups

230 Participants
are divided into 2 treatment groups

Sponsors and collaborators